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dc.contributor.authorManiruzzaman, M
dc.contributor.authorNokhodchi, A
dc.date.accessioned2018-08-26T07:20:36Z
dc.date.available2018-08-26T07:20:36Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/45943
dc.description.abstractCurrently, because globalization, the pharmaceutical industry is facing enormous challenges to comply with regulatory matters. Reduced patent life and overall decreased profitability of newly discovered drugs are also forcing the pharmaceutical industry to shorten the drug development time with maximum throughput. Therefore, continuous manufacturing (CM) processes via hot melt extrusion (HME) can be a promising alternative for achieving these goals. HME offers solvent-free green technology with a process that is easy to scale up. Moreover, CM provides better product quality assurance compared with batch processes, with fewer labor costs and shorter time to development. In this review, we primarily focus on various aspects of CM and the emerging application of HME to bridge the current manufacturing gap in pharmaceutical sphere.
dc.language.isoEnglish
dc.relation.ispartofDRUG DISCOVERY TODAY
dc.titleContinuous manufacturing via hot-melt extrusion and scale up: regulatory matters
dc.typeReview
dc.citation.volume22
dc.citation.issue2
dc.citation.spage340
dc.citation.epage351
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1016/j.drudis.2016.11.007


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